A.N. Belozersky Institute of M.V. Lomonosov Moscow State University, Moscow, Russia.
Cell Adh Migr. 2010 Jan-Mar;4(1):32-8. doi: 10.4161/cam.4.1.10314. Epub 2010 Jan 14.
In the present work, we demonstrate that microbial alkaloid staurosporine (STS) and Ro 31-8220, structurally related to STS protein kinase C inhibitor, caused development of membrane tubular extensions in human neutrophils upon adhesion to fibronectin-coated substrata. STS-induced tubular extensions interconnected neutrophils in a network and bound serum-opsonized bacteria Salmonella enterica serovar Typhimurium. The diameter of STS-induced extensions varied in the range 160-200 nm. The extensions were filled with cytoplasm and covered with membrane, as they included fluorescent cytoplasmic and lipid dyes. Neither protein kinase C inhibitors H-7 and bisindolylmaleimide VII, nor tyrosine protein kinase inhibitors tyrphostin AG 82 and genistein caused such extensions formation. Supposedly, STS induces membrane tubular extension formation promoting actin cytoskeleton depolymerization or affecting NO synthesis.
在本工作中,我们证明微生物生物碱星形孢菌素 (STS) 和结构上与 STS 蛋白激酶 C 抑制剂相关的 Ro 31-8220,在人嗜中性粒细胞黏附到纤维连接蛋白包被的基底上时,引起细胞膜管状延伸的发育。STS 诱导的管状延伸在网络中连接嗜中性粒细胞,并结合血清调理的细菌肠炎沙门氏菌血清型 Typhimurium。STS 诱导的延伸的直径在 160-200nm 范围内变化。延伸充满细胞质并覆盖有膜,因为它们包含荧光细胞质和脂质染料。蛋白激酶 C 抑制剂 H-7 和双吲哚马来酰亚胺 VII ,以及酪氨酸蛋白激酶抑制剂 tyrphostin AG 82 和金雀异黄素都不会引起这种延伸的形成。据推测,STS 诱导细胞膜管状延伸的形成,促进肌动蛋白细胞骨架解聚或影响 NO 合成。